A Study to Evaluate Changes in Human Breast Cancer Tissue Following Short-Term Use of Darolutamide

EARLY_PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

September 5, 2017

Primary Completion Date

February 14, 2019

Study Completion Date

March 13, 2019

Conditions
Breast Cancer Female
Interventions
DRUG

darolutamide

Oral 300 mg tablets; 600 mg (2 x 300 mg tablets) taken twice per day, to a daily dose of 1200 mg.

Trial Locations (14)

32806

UF Health Cancer Center - Orlando Health, Orlando

72076

Department of Women's Health, Tübingen

80336

Interdisziplinares Onkologisches Zentrum, München

90277

Torrance Memorial Physician Network, Cancer Care Associates, Redondo Beach

91054

Universitatsklinikum Erlangen, Erlangen

91405

Valley Breast Care and Women's Health Center, Los Angeles

93454

Central Coast Medical Oncology, Santa Maria

90095-1678

UCLA, Los Angeles

T6G1Z2

Cross Cancer Institute, Edmonton

H1T 2M4

(CIUSSS) de l'Est-de-l'Île-de-Montréal - l'Hôpital Maisonneuve-Rosemont, Montreal

H2X 3E4

Centre Hospitalier de l'Université de Montréal (CHUM), Montreal

H3T1E2

Jewish General Hospital, Montreal

H4A 3J1

McGill University Hospital, Montreal

G1S 4L8

Centre Hospitalier Affilie Universitaire De Quebec - Hospital Du Saint-Sacrement, Québec

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bayer

INDUSTRY

lead

Translational Research in Oncology

OTHER